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Synthesis of Jiamidogeru agent by using the amino acid N- carboxy anhydride

机译:氨基酸N-羧酐合成佳米多格鲁剂

摘要

The present invention provides a process for the synthesis of a compound according to formula I, comprising the following steps: a) reacting an N-carboxy anhydride according to formula II and an N-carboxy anhydride according to formula III with a diamine according to formula IV; and b) adding an acid to the reaction to adjust the pH value of the reaction to 7, wherein L is a C2-C20-alkyl group, C6-C20-aryl group, or C7-C20- Represents an alkylaryl group, and R1 and R2 may be the same or different, and are a hydrogen atom, a C1-C6-alkyl group, a C1-C4-hydroxyalkyl group, a C1-C4-thioether group, a C6-C20- An aryl group, a C7-C20-alkylaryl group, a C7-C20-alkylhydroxyaryl group, a C4-C20-alkylheteroaryl group having 1-4 heteroatoms, or a C1-C4-a Kirukarubokishi component represents the (acid, or may be an amide, or C1~C6- alkyl group or C7~C20- alkylaryl group may be esterified), relates to the aforementioned method.
机译:本发明提供了一种合成根据式I的化合物的方法,该方法包括以下步骤:a)使根据式II的N-羧酸酐和根据式III的N-羧酸酐与根据式I的二胺反应IV; b)向反应中加入酸以将反应的pH值调节至<7,其中L为C2-C20烷基,C6-C20芳基或C7-C20-代表烷基芳基,并且R 1和R 2可以相同或不同,并且是氢原子,C 1 -C 6烷基,C 1 -C 4羟烷基,C 1 -C 4硫醚基,C 6 -C 20芳基, C 7 -C 20烷基芳基,C 7 -C 20烷基羟基芳基,具有1-4个杂原子的C 4 -C 20烷基杂芳基或C 1 -C 4 -Kirukarubokishi组分代表(酸,或者可以是酰胺,或C 1 -C 6-烷基或C 7 -C 20-烷基芳基可被酯化),涉及前述方法。

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